A curated catalogue of human genomic structural variation




Variant Details

Variant: essv19411



Internal ID9956933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45526265..45931516hg38UCSC Ensembl
Innerchr10:46021713..46426964hg19UCSC Ensembl
Innerchr10:45341719..45746970hg18UCSC Ensembl
Innerchr10:45341719..45746970hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38405252
hg19405252
hg18405252
hg17405252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758217
Supporting Variants
SamplesNA11840
Known GenesAGAP4, FAM21C, MARCH8, ZFAND4
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv19411
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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